A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17021652



Internal ID82087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16804966..16818337hg38UCSC Ensembl
chr9:16804964..16818335hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3813372
hg1913372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485799
Supporting Variants
Samples
Known GenesBNC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17021652
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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